69775-51-5

Basic information

• Product Name: 2-Hydroxy-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene
• Synonyms: 2-Hydroxy-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene;5,8-diMethoxy-1,2,3,4-tetrahydronaphthalen-2-ol
• CAS NO: 69775-51-5
• Molecular Formula: C₁₂H₁₆O₃
• Molecular Weight: 208.25364
• Mol File: 69775-51-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Density: 1.148±0.06 g/cm3 (20 ºC 760 Torr)
• CAS DataBase Reference: 2-Hydroxy-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Hydroxy-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene(69775-51-5)
• EPA Substance Registry System: 2-Hydroxy-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene(69775-51-5)

Safety Data

• Hazardous Substances Data: 69775-51-5(Hazardous Substances Data)

Upstream product

• 106-51-4 p-benzoquinone 
• 858458-53-4 3-ethoxy-5,8-dimethoxy-1,2-dihydro-naphthalene 
• 66947-66-8 (+/-)-6-ethoxy-(4ar,8ac)-4a,5,8,8a-tetrahydro-[1,4]naphthoquinone 
• 69031-41-0 2-ethoxy-5,8-dimethoxy-1,4-dihydro-naphthalene 
• 143406-79-5 (2S,3S)-3-[(2-Hydroxy-ethyl)-methyl-amino]-5,8-dimethoxy-1,2,3,4-tetrahydro-naphthalen-2-ol; hydrochloride 
• 143325-80-8 N-oxide of trans-3-(N-hydroxyethyl-N-methylamino)-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthol 
• 58851-64-2 6,7-epoxy-5,6,7,8-tetrahydro-1,4-dimethoxynaphthalene 
• 37464-90-7 5,8-dimethoxy-2-tetralone 

Downstream Products

• 37464-90-7 5,8-dimethoxy-2-tetralone 

Relevant articles and documents

THE SYNTHESIS AND IDENTIFICATION OF ISOMERIC PRODUCTS OF ENZYMATIC O-DEMETHYLATION OF THE SYMPATHOMIMETIC TETRAMINOL - trans-3-(2-HYDROXYETHYLAMINO)-5,8-DIMETHOXY-1,2,3,4-TETRAHYDRO-2-NAPHTHOL

The structure of the positional isomers of mono-O-demethylated metabolites (V and VI) of Tetraminol - trans-3-(2-hydroxyethylamino)-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthol (XIX) - and the pairs of related derivatives was determined.

P-aminophenols, derivatives thereof and method of use

p-Aminophenols are provided having the structure STR1 wherein m is 0, 1 or 2; n is 0, 1, 2 or 3; R1 and R2 may be the same or different and are H, hydroxy or alkoxy; R3 is H, lower alkyl, alkanoyl or aroyl and R4 is H, lower alkyl or alkanoyl, and including acid-addition salts thereof. These compounds are useful as inhibitors of leukotriene production and as such are useful as antiallergy, anti-inflammatory and anti-psoriatic agents.

A short, efficient synthesis of an anthracycline antitumor antibiotic synthon

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